Search

everythinglearnresearchcommunity

for

Search:↓

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

Wnt signaling is important for development and cell regulation but can cause diseases like cancer when not working properly.

Noncoding dsRNA boosts hair growth by activating TLR3 and increasing retinoic acid.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

Androgens significantly affect female hair loss, and hormonal treatments may help.

Birth control pills increase the risk of blood clots, especially within the first year and with certain types.

The conclusion is that androgen receptor gene polymorphism might be a marker for polycystic ovary syndrome, but more research is needed.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

The gene KAP22-1 affects wool yield and fiber shape in sheep.

Heparan sulfate is important for hair growth, preventing new hair formation in mature skin, and controlling oil gland development.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Distinct β-catenin patterns are linked to cell growth, not cell death, in lung cancer.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Neuroactive steroids show promise for treating mental and neurological disorders by targeting GABA_A receptors.

CRAC channels are crucial for the development and function of specialized immune cells, preventing severe inflammation and autoimmune diseases.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

FA2H is essential for normal fur and sebum production in mice.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Most patients with Porphyria Cutanea Tarda had skin blisters and were often affected by hepatitis C and alcohol abuse, with differences between familial and sporadic cases.

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

The review found no clear link between vitamin D receptor gene variations and polycystic ovary syndrome.

Skin and hair can regenerate after injury due to changes in gene activity, with potential links to how cancer spreads. Future research should focus on how new hair follicles form and the processes that trigger their creation.

New treatments for immune disorders caused by FOXN1 deficiency are promising.

Mice can correct hair follicle orientation without certain genes, but proper overall alignment needs those genes.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

High afamin levels are linked to metabolic syndrome and may predict its development in women with insulin resistance.

Cellular senescence has both cancer-blocking and cancer-promoting effects, and targeting senescent cells may improve health and lifespan.

Prominin-1 expressing cells in the dermal papilla help regulate hair follicle size and communication but don't aid in skin repair.

Loss of keratin K2 causes skin problems and inflammation.